Articles producció científica> Química Física i Inorgànica

Reactivity Trends with Borylalkyl Copper(I) Species

  • Dades identificatives

    Identificador: imarina:9219136
    Autors:
    Corro MSalvado OGonzález SDominguez-Molano PFernández E
    Resum:
    The renaissance on the application of gem-diborylalkanes from 2010, has allowed the conquest of new synthetic application towards C−C and C−N bond formation. The activation of gem-diborylalkanes by Cu(I) catalysts, generates active borylalky copper(I) species that are able to trap several electrophilic reagents, in an efficient way. In addition, the modification of Cu(I) complexes with chiral ligands, induces asymmetric platforms towards the synthesis of enantioenriched organoboron compounds.
  • Altres:

    Autor segons l'article: Corro M; Salvado O; González S; Dominguez-Molano P; Fernández E
    Departament: Química Física i Inorgànica
    Autor/s de la URV: Corro Morón, Macarena / Domínguez Molano, Paula / Fernández Gutiérrez, Maria Elena / González Morán, Sara / Salvadó Ruiz, Oriol
    Paraules clau: Α-boryl carbanions Enantioselectivity Electrophilic trapping Diastereoselectivity Copper Alpha-boryl carbanions Allylic substitution olefination gem-diborylalkanes esters enantioselectivity enantioselective synthesis electrophilic trapping diborylmethane diastereoselectivity diastereo copper aldimines aldehydes 1,1-diborylalkanes
    Resum: The renaissance on the application of gem-diborylalkanes from 2010, has allowed the conquest of new synthetic application towards C−C and C−N bond formation. The activation of gem-diborylalkanes by Cu(I) catalysts, generates active borylalky copper(I) species that are able to trap several electrophilic reagents, in an efficient way. In addition, the modification of Cu(I) complexes with chiral ligands, induces asymmetric platforms towards the synthesis of enantioenriched organoboron compounds.
    Àrees temàtiques: Química Medicina i Materiais Interdisciplinar Inorganic chemistry Farmacia Engenharias iii Engenharias ii Ciências biológicas ii Ciências biológicas i Chemistry, inorganic & nuclear Astronomia / física
    Accès a la llicència d'ús: https://creativecommons.org/licenses/by/3.0/es/
    Adreça de correu electrònic de l'autor: oriol.salvado@urv.cat paula.dominguez@urv.cat paula.dominguez@urv.cat sara.gonzalez@urv.cat oriol.salvado@urv.cat mariaelena.fernandez@urv.cat
    Identificador de l'autor: 0000-0002-7309-8956 0000-0001-9025-1791
    Data d'alta del registre: 2024-07-27
    Versió de l'article dipositat: info:eu-repo/semantics/publishedVersion
    Enllaç font original: https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejic.202100296
    URL Document de llicència: https://repositori.urv.cat/ca/proteccio-de-dades/
    Referència a l'article segons font original: European Journal Of Inorganic Chemistry. 2021 (28): 2802-2813
    Referència de l'ítem segons les normes APA: Corro M; Salvado O; González S; Dominguez-Molano P; Fernández E (2021). Reactivity Trends with Borylalkyl Copper(I) Species. European Journal Of Inorganic Chemistry, 2021(28), 2802-2813. DOI: 10.1002/ejic.202100296
    DOI de l'article: 10.1002/ejic.202100296
    Entitat: Universitat Rovira i Virgili
    Any de publicació de la revista: 2021
    Tipus de publicació: Journal Publications
  • Paraules clau:

    Chemistry, Inorganic & Nuclear,Inorganic Chemistry
    Α-boryl carbanions
    Enantioselectivity
    Electrophilic trapping
    Diastereoselectivity
    Copper
    Alpha-boryl carbanions
    Allylic substitution
    olefination
    gem-diborylalkanes
    esters
    enantioselectivity
    enantioselective synthesis
    electrophilic trapping
    diborylmethane
    diastereoselectivity
    diastereo
    copper
    aldimines
    aldehydes
    1,1-diborylalkanes
    Química
    Medicina i
    Materiais
    Interdisciplinar
    Inorganic chemistry
    Farmacia
    Engenharias iii
    Engenharias ii
    Ciências biológicas ii
    Ciências biológicas i
    Chemistry, inorganic & nuclear
    Astronomia / física
  • Documents:

  • Cerca a google

    Search to google scholar